Alpha-nicotinoyl phenylacetonitriles

ABSTRACT

The present invention concerns itself with Alpha -nicotinoyl phenylacetonitriles and derivatives thereof which are useful as chemical intermediates in the preparation of novel aza-dibenzo (a,d)cycloheptenes.

0 United States Patent 1191 [111 3,717,647

Villani 1451 Feb. 20, 1973 [54] ALPHA-NICOTINOYL [51] Int. Cl. ..C07d 31/46 PHENYLACETONITRILES [58] Field of Search ..260/294.9, 295 AM [75] Inventor: grpnk J. Villam, West Caldwell, 56] References Cited [73] Assignee: Schering Corporation, Bloomfield, UNITED STATES PATENTS NJ. 3,337,568 8/1967 Bencze et a1 ..260/295 AM [221 Filed 1971 OTHER PUBLICATIONS [21] App! 132882 Kulczynski et al., Chem Abstracts, Vol. 57, No. 7,

Related us. Application Data (1962) [63] Continuation-impart of Ser. No. 754,453, Aug. 21, P i E i Alan L, Rot an 1968, abandoned, which is a continuation-in-part of Attorney stephen Coan and Raymond A M Ser. N0. 580,213, Sept. 19, 1966, Pat. NO. 3,419,565, Donald which is a continuation-in-part of Ser. Nos. 330,244, Dec. 13, 1963, Pat. N0. 3,366,635, and Ser. No. 330,263, Dec. 13, 1963, Pat. N0. 3,326,924, which is [57] ABSTRACT a Continuation-impart 0f 275,237, April The present invention concerns itself with a-nicotinoyl 1963 abandoned phenylacetonitriles and derivatives thereof which are useful as chemical intermediates in the preparation of [52] US. Cl. ..260/294.9, 260/290 R, 260/295 R,

260/295.5 R, 260/297 R, 260/297 T, 424/263 novel aza-dibenzo [a,d]cycloheptenes.

5 Claims, No Drawings ALPHA-NICOTINOYL PHENYLACETONITRILES CROSS REFERENCES TO RELATED APPLICATIONS continuation-impart applications of Ser. No. 275,237,

filed Apr. 24, 1963, now abandoned.

One aspect of this invention relates to compositions described as aza-dibenzocycloheptenes, the tricyclic nucleus of which has the following structural formula:

f B Q wherein the dotted line represents an optional double bond; B, together with the carbon atoms to which it is attached, represents a fused pyridine ring; Q is a .member of the group consisting of hydrogen, hydroxy,

halogen, lower alkyl, lower alkoxy and trifluoromethyl, and Z is a member of the group consisting of wherein A is a member of the group consisting of piperidyl and W is a member of the group consisting of H and OH,

and D is a member of the group consisting of piperidylidene and LII The invention in another of its composition aspects is described as residing in the concept of pharmaceutically acceptable acid addition salts of the compounds embraced by Formula 1.

The invention in still another of its composition aspects is described as residing in the concept of valuable intermediates which thenselves are aza-dibenzocycloheptadienes, the tricyclic nucleus of which has the following structural formula:

wherein the definitions for B, Q and the dotted line are the same as defined for Formula 1 above, and O is a member of the group consisting of (H,H) and O.

The novel compounds of Formula I are in essence final products, although as it will be later described, some of. these final products have the additional utility of being intermediates in the preparation of other final products.

The nomenclature employed herein is that approved by Chemical Abstracts, 1959, for dibenzocycloheptenes. The identification of the positions in the tricyclic system is exemplified by the following molecular structure for 4-aza-5-(N-methyl-4-piperidylidene)-l0,1 1- dihydro-5H-dibenzo[a,d]-cycloheptene, a member of the 4-aza series:

l CH3 Embraced within the composition aspect of the concept as represented by Formula I are the l-aza, 2-aza, 3-aza, and 4-aza-analogs all of which fall within the definition of B as a fused pyridine ring. It is apparent that the compounds of Formula I are amines attached to an aza-dibenzocycloheptene nucleus at the S-position through a hydrocarbon connecting link. By way of further definition, those compounds falling within Formula I, wherein W represents hydroxy, are sometimes called hydroxy compounds or carbinols, those wherein W represents hydrogen are sometimes called saturated compounds and those having the doubly bound substituent, D, are sometimes called unsaturated compounds" or alkylidene compounds.

The substituent A, as described herein includes a limited number of amino-hydrocarbyl substituents. Within the definition of A is the substituent piperidyl which includes 3-piperidyl, 4-piperidyl-, N-lower alkyl (preferably methyl) -3-piperidyl, N-lower alkyl (preferably methyl)-4-piperidyl. Included within the definition of A is the group ZO KDQ with X being defined as a hydrocarbyl group having two to nine carbon atoms. Representative of such groups are straight and branched hydrocarbon radicals of which ethyl, propyl, butyl, pentyl, octyl, phenylgroup. This context should be applied throughout in the designation ofthe hydrocarbyl and hydrocarbylidene substituent.) Also embraced within the term X are cyclic hydrocarbyl groups such as represented by cyclohexyl, cyclohexylmethyl and the like.

The substituent D is a doubly bound group identical to the piperidyl grouping and XNR,R, grouping in A except that the carbon atom of the substituent directly attached to the -position of the tricyclic nucleus has one less hydrogen atom and is doubly bound to said position. Embraced within the definition of D are piperidylidene (3-piperidylidene, 4-piperidylidene, N-methyl-3- and 4-piperidylidene) lower hydrocarbylidene having two to nine carbon atoms such as ethylidene, propylidene, cyclohexylidene, phenylpropylidene and other ylidene analogs of X.

The substituent includes amino, lower alkyl amino (preferably methylamino) and lower di-alkylamino (preferably dimethylamino). The scope of includes those tertiary amino groups wherein R and R,

tached form a heterocycle having live to six cyclic atoms, one of said cyclic atoms, other than the aforesaid nitrogen atom, being selected from the group together with the nitrogen atom to which they are atconsisting of C, O, and N and all other cyclic atoms being carbon. This aspect includes, pyrrolidino, piperidino, morpholino, piperazino (the last being inclusive of 4-methylpiperazino, 4-(2-hydroxyethyl)- piperazino, 4-(hydroxy-lower alkoxy)-piperazino and the like).

Compounds having the general Formula I also include those possessing a substituent in the benzenoid portion of the nucleus. These substituents are preferably located in the 7 and/or 8-po'sition. The substituent is generally one that does not usually provide for a difference in the kind of physiological property exhibited by the corresponding unsubstituted compound, the difference being rather in degree. Such substituents include lower alkyl, preferably methyl, halogen, preferably chlorine or bromine, pseudo halogen-like trifluoromethyl, hydroxy and lower alkoxy. These benzenoid substituted compounds are considered to be essentially the equivalents of their unsubstituted analogs andas such are fully contemplated as being within the scope of this invention.

The compounds contemplated as falling within Formula l are basic in character and form acid addition salts with acids. These salts sometime increase solubility and lend themselves better to formulation than do the free bases. Accordingly, the pharmaceutically ac ceptable acid addition salts of the free bases are contemplated as being within the concept in its composition aspect. Such salts include those derived from maleic, salicylic, succinic, methyl sulfonic, tartaric, citric, hydrochloric, hydrobromic, sulfuric phosphoric and the like.

The novel compounds of this invention represented by Formula I are characterized by their antihistaminic, anti-serotonin and antianaphylactic action and are useful in the treatment of allergic disorders such as urticaria, seasonal rhinitis and pollen sensitivity.

Within the classes of compounds encompassed by this invention i.e. the carbinols, the saturated compounds and the alkylidene compounds of each of the laza, 2-aza, 3-aza and 4-aza series), some appear of greater therapeutic utility than others. Although all of the compounds possess the above described properties, there are certain structure activity relationships pertaining to potency and utility. For example, the 4-aza compounds appear more potent than the other position isomers as antihistaminic substances. The piperidylidene compounds appear more potent than dimethylaminopropylidene as antihistaminic agents, but the latter group appears to be of greater interest in their effect upon the central nervous system. Compounds having the 3-aza grouping appear also to exhibit antihypertensive properties. The hydroxy compounds and the saturated compounds appear to exhibit properties similar to the alkylidene cogeners but to a lesser extent. Those compounds which are unsaturated at position 10 and l 1 appear somewhat less potent than their saturated analog.

The novel compounds described herein are administered in pharmaceutical formulations comprising the substance in admixture with a pharmaceutical carrier suitable for enteral or parenteral administration. The formulations may be in solid form as for example tablets and capsules or in liquid form as for example syrups, elixirs, emulsions, and injectables. In the formulation of pharmaceutical dosage forms there generally is utilized excipients as for example, water, gelatin, lactose, starches, magnesium stearate, talc, vegetable oils, benzyl alcohols, gums, polyalkylene glycols, and petroleum jelly.

In one of its process aspects, the invention sought to be patented resides in the concept of producing a compound of Formula I by reacting a S-keto-aza-dibenzocycloheptene with an organometallic compound bearing an amino substituted group embraced by the substituent A and hydrolyzing the complex thereby formed. The organometallic reactant may be a Grignard type reagent such as N-methyl-4-piperidyl magnesium halide (or zinc halide), preferably chloride or bromide. This step may be summarized by the following reaction sequence:

' binols of Formula I (or VI) wherein the substituent A contains at least three carbon atoms separating the amino group from the 5-position of the tricyclic nucleus. Any free amino group, such as a primary or secondary amine, must be protected prior to formation of the organometallic reactant in order to prevent these groups from reacting with the metallo-organic reagent. I prefer to protect free amine groups with benzyl. The carbinol so formed will accordingly contain the benzyl blocking group which is easily cleaved by catalytic hydrogenation to regenerate the corresponding amine.

In a preferred procedure, a S-keto-aza-dibenzocycloheptene (IV) is added either in solid form or in solution in an inert solvent to a Grignard reagent containing the substituent A which is also in suchan inert solvent such as, for example, ether, benzene, tetrahydrofuran and the like. Representative of the organometallic reactant are N-methyl-4-piperidyl magnesium chloride, dimethylaminopropyl magnesium chloride, and the like which are prepared in a known manner from magnesium and the corresponding amino alkyl halide. The reaction mixture may be heated, preferably under reflux, after which time it is subjected to hydrolysis. Hydrolysis under practically neutral conditions such as is effected by ammonium chloride results in formation of the carbinol (Vl) which is isolated from the reaction mixture by extraction with a water-immiscible solvent such as ether, chlorinated hydrocarbons and the like. The carbinols of Formula I, may be utilized as such or in the form of their acid addition salts.

The carbinols are valuable intermediates in the production of the unsaturated compounds of Formula produce an exocyc lic unsaturated compound of Formula I. The dehydration may be effected by heating the carbinol with known dehydrating agents such as alcoholic hydrogen chloride, phosphorous oxychloride, 5 phosphoric acids such as polyphosphoric acid, sulfuric acid, zinc chloride, alkali pyrosulfate and other similarly acting agents. These unsaturated products (wherein Z or Formula I represents C=D) may be isolated as free bases or in the form of their acid addition salts. The piperidylidene compounds of this class are particularly useful in the treatment of allergies. Thus, the dehydration of the carbinols to produce the corresponding unsaturated analog represents a further aspect of the process concept of the invention sought to be patented.

A further utility of the exocyclically unsaturated compounds described above is that wherein they serve as intermediates in the preparation of the saturated compounds of Formulal (wherein Z represents are also preparable by direct alkylation of an azadibenzo-cycloheptene according to the following reaction scheme:

i ACl B Q 2151C (Oll cnsing agents II II II A \']1 VIII In the foregoing reaction scheme, the substituents A,

B, Q and the dotted line have the same meaning as 6 described heretofore. This reaction constitutes the condensation of an organic halide (preferably chloride or bromide) bearing the substituent A, with an appropriate aza-dibenzocycloheptene (VII). The reaction is carried out in an inert solvent such as toluene or xylene, preferably at reflux temperature, and in the presence of a condensing agent such as sodamide or potassium amide. Representative of the halides which may be used in this reaction are dimethylaminopropyl chloride, dimethylaminoethyl chloride and the like. The reaction product is obtained by neutralization of the mixture with mineral acid, followed by treatment with aqueous alkali and extraction with a water immiscible solvent. This method permits the production of saturated compounds (wherein Z represents In the foregoing reaction, B, Q and the dotted line have the same significance as ascribed heretofore. The reaction is effected in an inert solvent such as refluxing toluene of xylene and the product, 1X, separated therefrom according to methods well known in the art. The ester, IX, is then subjected to dehydration such as by heating with thionyl chloride to afford the exocyclically unsaturated analog, X, which is saponified by treatment with acid or alkali to yield the carboxylic acid, XI. The carboxylic acid, XI, is converted into an amide, XII, by first forming the acid chloride by means of thionyl chloride, followed by reaction with the amine I-INR 12,. This sequence of reactions is depicted in the following scheme and for convenience only the S-position of the tricyclic system is shown: v

dehydration C III.) 0.1120000215 saponlllcation (j JHzC O O C2115 150 C12 C v C II i N r 'i l1 CHCO 0H CHCONRIRZ XI XII In this reaction sequence, NR, R; has the same significance as ascribed heretofore but is preferably a tertiary amino group. Selective reduction of the amide group by means of lithium aluminum hydride, for example, yields the amino alkylidene, XIII, which may be further saturated to yield the aminoalkyl, XIV, by catalytic hydrogenation with palladium.

XII XIII XIV Compounds XIII and XIV are representative. of those of Formula I having two carbon atoms separating the amino group NR R from the 5-position of the tricyclic nucleus. The last step, that is the catalytic hydrogenation, is not selective and in addition to saturating the exocyclic double bond will also hydrogenate a 10,1 l-double bond if such is present.

It is apparent that key intermediates in the synthesis of compounds of Formula I are those azadibenzocycloheptenes having a tricyclic nucleus represented by Formula II. Embraced within this representation are l-aza-S H-dibenzo[ a,d lcycloheptene, 2-azaa5l-ldibenzo[a,d]cycloheptene, 3aza-5H-dibenzo[ a,d]cycloheptene, 4-aza-5H-dibenzo[a,dlcycloheptene, their 10,11-dihydro analogs, the S-keto analog of the foregoing and those containing a further substituent in the benzenoid ring as described heretofore. Representative of this latter group are, for example, 4- aza-7-chloro-5Hdibenzo[a,d]cycloheptene, 4-aza-8- chloro-SH- dibenzo[a,d]cycloheptene, the S-keto analogs and the 10,1 l-dihydr'o derivatives of both; the corresponding 7- and 8-bromo analogs, 7- and 8- methyl analogs and the like.

The S-keto intermediates of Formula II (Q,==O) are prepared by a variety of procedures of which I prefer an intromolecular cyclization of an ortho-styryl or orthophenethyl)-pyridine carboxylic acid according to the. following scheme:

XV IV In the foregoing scheme B, Q and the dotted line have Gory-Cir L A XVI XVII Q being as defined above. Similarly by starting with 4- styryl (or 4-phenethyl)-3-pyridyl carboxylic acid (X- VIIIa), the corresponding 3-aza ketone (IV) is produced; from 3-styryl (or 3-phenethyl)-4-pyridyl carboxylic acid (XVIIlb) there is obtained the 2-aza ketone (IV) and from 2-styryl (or 2-phenethyl)-3- pyridine carboxylic acid (XVIIIc) there is obtained the l-aza ketone (IV).

The cyclization as depicted above is effected on the pyridine carboxylic acid (XIV). Alternate and equivalent methods are readily apparent to one skilled in the art such as an intramolecular Friedel-Crafts reaction. By this method, the carboxylic acid is first converted to its acid chloride such as by means of thionyl chloride (or phosphorus trichloride or oxalyl chloride, for example) followed by treatment with aluminum chloride whereby cyclization occurs resulting in the formation of IV. The cyclization is carried out generally according to standard techniques for effecting a Friedel-Crafts reaction, namely heating the mixture in an inert solvent such as carbon disulfide, petroleum ether, benzene and the like and isolating the cyclized product therefrom.

The phenethyl pyridine carboxylic acids (XV) may be prepared by catalytic hydrogenation of the corresponding styryl pyridine carboxylic acids or by independent synthesis as set forth later herein. In certain instances as will be shown, the cyclic ketone (IV) having an unsaturation between positions 10 and ll sometimes are preferably prepared from the 10,1 l-dihydro analog by dehydrogenation with selenium dioxide or other methods equivalent in its results.

The reaction between benzaldehyde and ethyl 2- methyl nicotinate is carried out in refluxing acetic anhydride and gives rise to 3-carboxy-2-dihydrostilbazole lactone (XX). The lactone is converted directly into the cyclic ketone (XXIII) by heating with polyphosphoric acid. It may also be transformed indirectly via the stilbazole carboxylic acid (XXI) to the cyclic ketone (XXIII) as shown. Treating the lactone with phosphorus and iodine in water, or reducing the stilbazole carboxylic acid (XXI) yields 2-phenethyl nicotinic acid (XXII). This latter compound upon heating with polyphosphoric acid is transformed into the 10,1 l-dihydro analog of XXIII. I

In the foregoing reaction, chemical transformation of compound XIX to compound XX is old in the art but is shown herein to establish a basis for preparing the cyclic ketone (XXIII) and its l0,ll-dihydro analog wherein said ketone contains a substituent in its benzenoid portion. It should be apparent to one skilled in the art that these substitution analogs are prepared by using the appropriately substituted benzaldehyde. For example, if a benzaldehyde substituted in the para position, by a member represented by chlorine, bromine, trifluoromethyl, methyl, and the like, were used in the reaction, the correspondingly substituted lactones and 0000111,. -#()H7CN NaOCZHs l i Q XXIV XXV 0 (.N i-cn 1| IIBY- XXVI o Hl-CIL N Wolff- J Q Kislnmr XXVI] N S00: N

i Q U Q Pyridine XXVIll XXIX,

UV Q XXX In this reaction sequence, ethyl 4-methyl nicotinate (XXIV) is condensed with a phenylacetonitrile (XXV), preferably by means of sodium alkoxide (ethoxide) in ethanol giving rise to the keto nitrile (XXVI). Conversion of the ketone, XXVII, is effected by heating the keto nitrile with a strong mineral acid, preferably concentrated hydrobromic acid. Alternatively, this step may be effected by heating the keto nitrile with concentrated sulfuric acid whereby the nitrile is transformed into a carboxamide group. This is hydrolyzed and the product decarboxylated by adding water to the reaction mixture and continuing the heating operation. Reduction of the 3-pyridyl ketone, XX- VII, is preferably carried out by the well-known Wolff- Kishner reaction which involves heating the ketone with hydrazine hydrate in a high boiling polar solvent such as trimethylene glycol in the presence of alkali, such as sodium or potassium hydroxide. This reduction gives rise to a 3-phenethyl-4-methyl pyridine, XXVIII. This latter compound, upon oxidation with selenium dioxide in pyridine, for example, produces a 3- phenethyl-iso-nicotinic acid (XXIX) which, upon heating with polyphosphoric acid, undergoes cyclization to form the cyclic ketone, XXX. It is also apparent from this reaction scheme that cyclic ketones having the nucleus shown by compound XXX may be prepared, said compounds also having a further substituent such as chlorine, bromine, trifluoromethyl, methyl, and the like, in the benzenoid portion. In order to obtain such substituted compounds, the appropriately substituted phenylacetonitrile is employed. It is apparent that the use of a para-substituted phenylacetonitrile will ultimately give rise to the cyclic ketone, XXX, having said substituent in the 7-position. With a meta-substituted phenylacetonitrile, a mixture of ketones is obtained, one having the substituent in the 6-position and the other having the substituent in the 8-position. These may be separated either at this final step or the isomeric intermediates may be separated at any one of the steps of the reaction sequence by standard techniques, such as fractional distillation, fractional crystallization, column chromatography, and the like.

The 10, ll-dehydro analog of compound XXX is preferably prepared from compound XXX itself by dehydrogenation as effected by selenium dioxide in pyridine or by treating compound XXX with N-bromsuccinimide and then dehydrobrominating the so formed bromo intermediate.

In order to prepare the 3-aza-ketones of Formula IV, the following sequence of reaction is preferred:

Q being as defined above.

In this reaction sequence, ethyl 4-rnethyl nicotinate, the same starting substance as used in the 2-aza series, is reacted with benzaldehyde in refluxing acetic anhydride giving rise to the stilbazole carboxylic ester, XXXI. Reduction of this ester catalytically, such as with palladium and hydrogen, followed by hydrolysis of the ester group, produces 4-phenethyl nicotinic acid (XXXII). which upon heating with polyphosphoric acid, is cyclized to form the 3-aza-ketone, XXXIII. Here again, the 7-chloro-, 7-bromo-, 7-trifluoromethyland 7-rnethyl-substituted ketones are readily prepared by utilizing the appropriately para-substituted benzaldehyde.

The 10,11-dehydro analogs of XXXIII are prepared either by dehydrogenation of the ketone itself as described heretofore, or by hydrolyzing the stilbazole carboxylate, XXX], to the corresponding carboxylic acid and then heating said acid with polyphosphoric acid. If the cyclization is carried out at elevated temperatures in the range of 190C, there is predominantly obtained the 10,11-dehydro analog of XXXIII. At lower temperatures, a side product, namely, the lactone of 3-carboxy-4-dihydro stilbazole is formed. This lactone, when heated with polyphosphoric acid according to the procedure described for the l-aza series, is transformed into the cyclic ketone. To prepare the 4- aza-ketones of Formula IV, I prefer to utilize the following sequence of reactions:

7 same sequence of reactions. described for the prepara- Q being as defined above. In this sequence, a nicotinic acid ester, preferably ethyl nicotinate (XXIV), is converted into a 3-phenethyl pyridine (XXXVII) by the tion of the 2-aza-ketones. The condensation with a phenylacetonitrile is preferably carried out in' ethanol in the presence of sodium ethoxide; however, other condensation agents may also be used, such as sodamide or sodium hydroxide in a benzene or toluene solvent. In place of the Wolff-Kishner reduction, there may also be employed copper chromite in dioxane at about C under about 1500 lbs. pressure of hydrogen. The phenethyl pyridine (XXXVII) is transformed into its N-oxide (XXXVIII) by means of a peroxy acid, such as hydrogen peroxide and acetic acid. Reacting this oxide in turn with dimethyl sulfate and then aqueous sodium cyanide gives rise to 3- phenethyl-Z-pyridyl-nitrile, XXXIX. The nitrile is cyclized directly to the 4-aza-ketone, XL, by heating with polyphosphoric acid or it may first be hydrolyzed to the corresponding carboxylic acid, XLI, and then cyclized. In this synthesis, compounds analogous to XL and having a benzenoid substituent are prepared by utilizing the appropriately substituted phenylacetonitrile. The

10,1 l-dehydro analog of XL may be prepared by direct dehydrogenation with selenium dioxide in pyridine, for example, or by any of the methods set forth in the examples which later follow.

3-Phenethylpyridine-N-oxide (XXXVIII) is especially valuable in preparing the 4-aza ketone XL in that other transformations may be effected giving rise to the cyclic ketone. In particular, reacting the N-oxide with acetic anhydride gives rise to 2-acetoxy-3-phenethyl pyridine (XXXVIIla) which is hydrolyzed to the 2- hydroxy analog (XXXVIIIb) by means of aqueous mineral acid, e.g., hydrochloric acid. The hydroxy group is replaced by bromine (by means of phosphorous oxybromide) to yield the 2-bromo-3- .phenethylpyridine (XXXVIIIc). Reaction of this latter intermediate with butyl lithium and then with carbon dioxide results in the formation of the carboxylic acid (XLI) which is then cyclized.

It is apparent to one skilled in the art that there are innumerable variations of the foregoing reactions which produce phenethyland styryl-pyridine carboxylic acids, all of which are deemed chemically equivalent to those depicted. Indeed any phenethylor styryl-pyridine having a carboxyl (or a group convertible thereinto) in a position adjacent to the phenethyl (or styryl) group is a potential and valuable intermediate for producing the aza-dibenzocycloheptenones. Further, various aspects of the processes depicted are interchangeable to the extent that the pyridine has the appropriate substitution. For example, the reaction scheme for preparing the 2-aza-ketone, XXX, can be adapted to prepare the 4-aza-ketone (XL) merely by using ethyI-Z-methyl nicotinate as starting material. The close analogy between the methods for preparing the l-aza-ketone (XXIII) and the 3-aza-ketone (XXXIII) is readily apparent. Accordingly, this invention is not particularly concerned with the preparation of phenethyl (or styryl)-pyridine carboxylic acids themselves but is concerned with the cyclization of such compounds and their equivalents into aza-dibenzo-cycloheptenones.

The preparation of the aza-dibenzocycloheptenes, i.e., those compounds of Formula II wherein Q represents (H,I'I), is accomplished. by any of the known methods for converting a keto group to a methylene group. The Wolff-Kishner reduction technique wherein the ketone is treated with hydrazine and potassium hydroxide whereby the carbonyl function is converted ,to a methylene group is the preferred method. On the otherhand, the ketone may first be reduced to the corresponding carbinol which, in turn, is further reduced to methylene. This can be effected by reacting the ketone with lithium aluminum hydride, with zinc dust in ammonia, or by catalytic reduction using platinum oxide or Raney Nickel. The carbinols may be converted to the methylene by ehlorinating with thionyl chloride and then replacing the chlorine atom with hydrogen by refluxing the chloro-intermediate in the presence of zinc dust, potassium iodide and acetic acid. The carbinols may be directly reduced such as with iodine and phosphorus in glacial acetic acid. Other methods, of course, would be available. In those instances wherein the aza-dibenzo-cycloheptene-S-one intermediate contains the halogeno or trifluoromethyl, substituents in the benzenoid moiety, it is preferred to apply the .Wolff-Kishner reduction technique.

The foregoing descriptions relating to the preparation of the novel compounds of Formula I all utilize a key intermediate of Formula II as an immediate or near immediate precursor. In these afore-described syntheses the substituents A, W, and D are in essence added into an existing tricyclic system by reaction at the 5-position.

The following examples are illustrative of the product and process aspects of the invention sought to be patented. No meaning as to limitation of the invention is to be ascribed to the example.

PREPARATION OF KEY INTERMEDIATES Preparation A. l-aza-10,l l-dihydro-SI-I-dibenzo- [a,d]-cycloheptene-5-one and l-aza-5I-I-dibenzo-[a,d]- cycloheptene-5one.

Step 1. 2-(2-hydroxyphenethyl)-nicotinic lactone hydrochloride:

Stir and reflux a mixture of 65 g. ethyl 2-methylnicotinate, 57 g. benzaldehyde and 37 ml. acetic anhydride for 20 hours. Cool and pour the mixture into 2.0 N hydrochloride acid. After crystallization, filter and recrystallize the solid from ethanol obtaining 13.5 g. of 2-(2-hydroxyphenethyl nicotinic lactone) hydrochloride, M.P. 183l85C.

Step 2. 2-stilbazole-3-carboxylic acid: Admix 60 g. of red phosphorous, 20 g. of iodine in 1.5 l. glacial acetic acid and add in portions 176 g. of 2-(2-hydroxyphenethyl)-nicotinic lactone hydrochloride. Reflux for 20 hours and filter the hot solution through a sintered glass funnel. Pour the filtrate into water and filter 4 the precipitate after allowing time for formation and 40 Step 3. 2-phenethyl nicotinic acid:

coagulation. Dissolve the precipitate in 2 l. of warm dilute ammonium hydroxide (10-15 percent). Filter, and neutralize the filtrate with acetic acid. Cool and filter the precipitated 2-stilbazole-3-carboxylic acid. Recrystallize from ethanol, M. P. 2l9-22lC. (130 g.).

In a shakertype hydrogenation (Parr), mix 22 g. of 2-stilbazole-3- carboxylic acid, 200 ml. of ethanol and 20 ml. of 25 percent aqueous sodium hydroxide. Hydrogenate the mixture at lbs. pressure of hydrogenusing freshly prepared Raney nickel catalyst. When thetheoretical amount of hydrogen is absorbed (1 mole per mole of acid), filter and concentrate the filtrate by heating on a steam bath. Dissolve the residue in water, acidify with acetic acid and filter the crude phenethyl nicotinic 50 acid. Recrystallize from benzene-hexane, M.P.

Alternatively, Z-phenethyl-nicotinic acid is prepared by heating gms. of the lactone (step 1) with 1 liter 57 percent hydriodic acid while adding 60 g. red phosphorous over a period of 2 hours. Reflux the mixture for 18 hours and filter while hot. Remove most of the excess hydriodic acid by concentration and neutralize the remaining solution with ammonium hydroxide whereupon 2-phenethylnicotinic acid precipitates. Step 4. l-aza-l0,l 1-dihydro-5H-dibenzo-[a,d]- cycloheptene-5-one: Admix 50 g. of Z-phenethylnicotinic acid and 500 g. of polyphosphoric acid and heat at -l65C., for 5-6 hours while stirring. Cool, pour the mixture into ice water and neutralize with ammonium hydroxide. Extract with ether. Wash the ether solution with 10 percent sodium hydroxide solution. Dry the ether layer and concentrate to a residue.

. [a,d]-cycloheptene--one Crystallize from hexane obtaining the ketone of this step, M.P. 62-64C.

Step 5. 1-aza-5H-dibenzo-[a,d,]-cycloheptene-5- one: Dissolve 20 g. of the ketone from step 4 in 150 ml. of acetic acid and add 40 ml. of 30 percent hydrogen peroxide. Heat in a water bath maintained at 65-70C. for 24 hours, and pour into ice water. Neutralize with concentrated sodium hydroxide solution and allow to crystallize. Filter, recrystallize from dilute ethanol and air dry, obtaining the N-oxide of the ketone of step 4. To 100 ml. of refluxing acetic anhydride, add 15 g. of the N-oxide prepared above. Reflux the mixture for hours, and then pour into water. Allow to stand several hours and then neutralize with sodium bicarbonate. Extract the mixture with chloroform and evaporate the chloroform extract to dryness. Treatthe residue with 100 ml. of 48 percent hydrobromic acid and 100 ml of acetic acid and then reflux the mixture for 6 hours. Concentrate in vacuo, dissolve the residue in water and make alkaline with ammonium hydroxide. Extract the mixture with ether. Concentrate the ether solution to a residue. Crystallize from petroleum ether, obtaining l-aza5l-l-dibenzo-[ a,d]cycloheptene-5-one, M.P. 95-96C.

Preparation B. 2-aza-10,11-dihydro-5l-l-dibenzo- [a,d]-cycloheptene-5-one and 2-aza-5l-l-Dibenzo-[ a,d]-cycloheptene-5-one Step 1. a-(4-methyl)-nicotinoyl-phenylacetonitril: Follow the procedure of Preparation D, step 1 using ethyl 4-methyl-nicotinate.

Step 2. Benzyl-3-(4-methyl)-pyridyl ketone: Using the product of step 1 follow procedure of Preparation D, step 2.

Step 3. 3-phenethyl-4-methylpyridine: Using the product of step 3, following the procedure of Preparation D, step 3.

Step 4. 3-phenethyl-isonicotinic acid: Reflux a mixture of 8.6 g., 3-phenethyl-4-methylpyridine, 50 ml. dry pyridine, and 12 g. powdered selenium dioxide for 3 hrs. Dilute with CHCl and filter. Evaporate filtrate to a residue. Dissolve residue in dilute ammonium hydroxide and extract with ether. Acidify the aqueous layer with acetic acid and filter. Recrystallize from isopropyl ether, obtaining 3.9 g., M.P. 99-101C.

Step 5 2-aza-l0,l 1-dihydro-'5H-dibenzo- [a,d]cycloheptene-5-one: Utilizing the acid from Step 4, heated with polyphosphoric acid as in Preparation A, step 4.

Step 6 2-aza-5H-dibenzo-[a,d]-cycloheptene-5-one: Dehydrogenate the ketone from step '5 by the procedure of Preparation D, Step 7.

Preparation C. 3-aza-l0,11-dihydro-5l-l-dibenzoand 3-aza-5H-dibenzo-[ a,d]cycloheptene-5-one Step 1. Ethyl 4-stilbazole-3-carboxylate: Stir and reflux a mixture of 165 g. of ethyl 4-methyl nicotinate, 106 g. of benzaldehyde and 1 liter of acetic anhydride for 4 hours. Pour onto ice, filter and recrystallize from benzene obtaining the ester of this step.

Step 2. 4-stilbazole-S-carboxylic acid: Reflux for 6 hours a mixture of 50 g. of the ester from step 1, 50 g. of potassium hydroxide, 50 ml. of water and 200 ml. of ethanol. Concentrate to remove the solvents and dissolve the residue in 200 ml. of water. Neutralize with acetic acid and allow the 4-stilbazole-3-carboxylic acid to crystallize, filter and dry.

Step 3. 4-phenethyl nicotinic acid: Hydrogenate 22 g. of 4-stilbazole-3-carboxylic acid according to the analogous procedure described in Preparation A, step Step 4. 3 -aza-10,11-dihydro-5l-l-dibenzo-[a,d]-

cycloheptene-S-one: Admix g. of 4-phenethyl nicotinic acid and 1 kg. of polyphosphoric acid and follow the analogous procedure of Preparation A, step 4. Recrystallize from benzene-petroleum ether, M.P. 66-67C. Step 5. 3 -aza-5H-dibenzo-[a,d]-cycoheptene-5-one: Admix 50 g. of 4-stilbazole carboxylic acid (from step 2) with 1 kg. of polyphosphoric acid and follow procedure of Preparation A, step 4. Recrystallize from benzene-hexane,M.P. 157-158C..- Preparation D. 4-aza-l0,l l-dihydro-SH-dibenzo- [a,d]-cycloheptene-5-one and 4-aza-5H-dibenzo-[a,d]- cycloheptene-S-one Step 1. a-nicotinoyl phenylacetonitrile: To a refluxing solution of 34 g. of sodium in 500 ml. of absolute ethanol, add dropwise, a mixture of 260 g. of ethyl nicotinate and 133 g. of phenylacetonitrile. After 4 hours, pour the mixture onto ice and extract with ether. Neutralize the aqueous phase with acetic acid and allow the product to crystallize. Filter, wash with water and air dry. The so-obtained a-nicotinoyl phenylacetonitrile, M .P. 137-141C. is used in the next step without further preparation.

Step 2. Benzyl 3 -pyridyl ketone: Reflux the nitrile from step 1 for 16 hours with 1.4 liters of concentrated hydrobromic acid. Pour the mixture over ice and allow to crystallize. Filter the hydrobromide salt, suspend the preparation in water and neutralize with sodium carbonate solution. Allow to crystallize, filter and air dry, yield 126 g., M.P. 53-56C.

Step 3. 3-phenethylpyridine: Admix 26 g. of the ketonefrom step 2, 11 g. of sodium hydroxide, 11 ml. of percent hydrazine hydrate and 175 ml. of diethylene glycol. Place the mixture in a still and heat at 235-240C. for 3-4 hours permitting distillation to occur at libitum. Cool and extract the mixture and the distillate with benzene. Wash the combined benzene extracts with water and distil in vacuo collecting that fraction boiling at -128C./l mm., 21 g.

Step 4. 3-phenethylpyridine N-oxide: Heat a mixture of 183 g. of 3-phenethylpyridine, 120 ml. of 30 percent hydrogen peroxide, and 300 ml. of glacial acetic acid for 20-24 hours at 60-65C. Pour into ice water and adjust the pH to 8-9 with ammoniumhydroxide. Filter and dissolve the precipitate in chloroform. Concentrate to a residue and precipitate with hexane obtaining -158 g., M.P. 82-89C.

Step 5. 2-cyano-3-phenethyl pyridine: While stirring, add 75.6 g. of dimethyl sulfate, dropwise, to 118.8 g. of 3-phenethyl-pyridine N-oxide. Heat the mixture at 85C for 3 hours. Cool and dissolve in 180 ml. of water. Add the aqueous solution dropwise to a stirred solution of 88.2 g. of sodium cyanide in 250 m1. of water, all under an atmosphere of nitrogen with the reaction temperature in the range of 0-5C. Stir for 6 hours at 0C.,

and then allow the mixture to warm to room temperature by standing overnight. Extract with chloroform, wash extracts with water and distil in vacuo, collecting that fraction boiling at l60-167C at 0.8 mm. (A higher boiling fraction, 190195C/l.5 mm., is the 4- cyano isomer which may be transformed into the 2-aza ketone (Preparation B) by the analogous method described hereing.)

Step 6. 4-aza-10,l1-dihydro-5H-dibenzo-[a,d]- cycloheptene-S-one: Stir and heat 99 g. of 2-cyano- S-phenethylpyridine and 5 kg. of polyphosphoric acid at 180C. for 20-24 hours. Pour onto ice, neutralize with 50 percent aqueous sodium hydroxide and extract with chloroform. Concentrate to a residue, triturate with hexane and filter obtaining the ketone of this step, M.P. 6873C.

Step 7. 4-aza-5H-dibenzo-[a,d]-cycloheptene-5- one: Reflux a mixture of g. of the ketone from step 6, 15 g. of selenium dioxide and 60 ml. of pyridine for 4 hours under nitrogen. Cool, filter and wash precipitate with ethanol. Combine filtrate and ethanol washings and concentrate in vacuo to a residue. Make filtrate alkaline with ammonium hydroxide and extract with chloroform. Wash chloroform solution with water and concentrate to a residue. Crystallize from isopropyl ether or benzenehexane, M.P. l18l19C.

The foregoing preparations set forth methods for synthesizing the ketones of Formula IV which are key intermediates in the preparation of final compounds of Formula I. All these preparations as shown give rise to an azadibenzocycloheptenone unsubstituted in the benzenoid ring. As stated heretofore, to prepare substituted ketones having a substituent at one of the 6,7,8 and 9 positions, one merely employs the appropriately substituted reactant. Preparations A and C employ v benzaldehyde as an initial reactant while Preparations B and D employed phenylacetonitrile. If these reactants are substituted, the substituent will appear in the benzenoid portion of the azadibenzocycloheptenone, the position dependent upon the position in the initial reactant. A para substituent in the initial reactant gives ultimate rise to a 7-substituted azadibenzocycloheptenone; an ortho substituent appears in the 9-position while a meta substituent gives rise to a mixture consisting of a 6-substituted and an 8-substituted azadibenzocycloheptenone. The initial reactant, the benzaldehyde or the phenylacetonitrile, may thus bear an o-, morpsubstituent such as methyl, chloro, bromo, trifluoromethyl, rnethoxy and the like and such substituent will appear in the aforementioned position of the azadibenzocycloheptenone. To separate the mixture of 6- and 8-substituted azadibenzocycloheptenones, I prefer column chromatography whereby the mixture is adsorbed on alumina and eluted with benzene-hexane fractions containing varying propor- Step D-la a-nicotinoyl-m-chlorophenylacetonitrile:

to a solution of sodium ethylate prepared by dissolving 6.9 g. of sodium metal in 100 ml. of absolute ethanol, add (in a dropwise fashion, under a nitrogen atmosphere and at reflux on a steam bath) a solution of 51.3 g. of ethylnicotinate and 36 g. of m-chlorophenylacetonitrile. Reflux the mixture for 4 hours and pour the resulting mixture into ice water. Extract the clear yellow solution with ether and discard the ether layer.

Acidify the resulting aqueous solution with acetic acid and allow the product to crystallize. Filter and air dry the crude product at l-179C which can be used directly in the next step without further purification. Similarly, by substituting the 36 g. of m-chlorophenylacetonitrile with 36 g. of p chlorophenylacetonitrile, 32.4 g. of p-fluorophenylacetonitrile, and 33 g. of pmethylphenylacetonitrile and by substantially following the foregoing procedure, there is produced anicotinoyl-p-chlorophenlacetonitrile, a-nicotinoyl-pfluorophenylacetonitrile and a-nicotinoyl-pmethylphenylacetonitrile, respectively. Step D-2a m-chlorobenzyl3-pyridyl ketone: Under reflux conditions heat a mixture containing 50 g. of the crude anicotinoyl-m-chlorophenylacetonitrile and 400 ml. of concentrated (48 percent) hydrobromic acid for 16-24 hours. Pour the resulting mixture into ice and allow to crystallize. Filter the crude hydrobromic acid salt and resuspend in water. Neutralize the suspension with sodium hydroxide (pl-l 8-9) and extract with chloroform. Wash the chloroform extracts with water, dry and distill the chloroform. The residue is triturated with petroleum ether and is allowed to recrystallize to produce m-chlorobenzyl-3-pyridyl ketone. In a similar manner by substituting the crude nitrile with equivalent quantities of a-nicotinoyl-p-chlorophenylacetonitrile, a-nicotinoyl-p-fluorophenylacetonitrile and anicotinoyl-p-methylacetonitrile and by substantially following the foregoing procedure, there is produced pmethylbenzyl-3-pyridyl. ketone, p-fluorophenyl-3-' pyridyl ketone, p-chlorophenyl-3-pyridyl ketone, respectively. Step D-3a m-chlorophenethylpyridine: Heat a mixture containing 23.8 g. of m-chlorobenzyl-3-pyridyl ketone, 11 g. of sodium hydroxide, 11 ml. of percent hydrogen hydrate and 175 ml. of diethylene glycol at 230-240C for 3-4 hours, distilling off the low boiling liquids. Cool and extract with benzene and wash the combined benzene extract solutions with water and distil the washed benzene extract taking the distillate of 130-l35C/l ml. to obtain m-chlorophenethylpyridine. Similarly, 3-p-chlorophenethylpyridine. 3-pfluorophenethylpyridine, 3-p-methylphenylpyridine are obtained from 33.8 g. of p-chloro-benzyl-3-pyridyl ketone, 32.4 g. of p-fluorobenzyl-3-pyridyl ketone and 31.6 g. of p-methylbenzyl-3-pyridyl ketone by conducting substantially the same procedure used for the obtention of m-chlorophenethylpyridine. Preparation E. 4-aza-10,l l-dihydro-Sl-l-dibenzo- [a,d]-cycloheptene Reflux a mixture of 40 g. of 4-aza-10,ll-dihydro-5H- dibenzo-[a,d]cycloheptene-5-one, 50 g. of potassium hydroxide, g. of hydrazine hydrate and 350 ml. of trimethylene glycol for 24 hours. Concentrate in vacuo to 30 percent volume and pour the residue into icewater. Extract with ether, wash the ether solution with water and concentrate to a residue. Crystallize from aqueous methanol.

In a similar fashion, by utilizing any of the ketones of Preparations A-D, and the substitution products thereof as described in the preceding passage, and reacting said ketones as above described, the corresponding azadibenzocycloheptene is obtained.

PREPARATION OF CARBINOLS Example 1. 4-aza-5(N-methyl-4-piperidyl)-10,1ldihydro-H-dibenzo[a,d]-cycloheptene-5-ol Add 17.4 g. of N-methyl-4-chloropiperidine to a stirred mixture containing 3.2 g. of magnesium, 20 ml. of anhydrous tetrahydrofuran, 1 ml. of ethyl bromide and a crystal of iodine. Reflux for two hours, cool to 30-35C. and add a solution of 13 g. of 4-azal0,l ldihydro-SH-dibenzo[a,d1-cycloheptene-5-one in 25 ml. of tetrahydrofuran. Stir for 5 hours, remove the solvent by distillation in vacuo and add 250 ml. of ether. Add 100 ml. of percent ammonium chloride solution and extra the mixture with chloroform. Concentrate the chloroform solution to a residue and recrystallize from isopropyl ether obtaining g. of the carbinol of this example, M.P. l731'74C.

By substituting the analogous aza-ketones in the foregoing (the l-aza, 2-aza, and 3-aza ketones). the corresponding carbinols are obtained.

Example 2. 1-aza-(5-dimethylaminopropyl)-10,lldihydro-5H-dibenzo[a,d]-cycloheptene-5-ol To a stirred mixture of 6.8 g. of magnesium, 150 ml. of anhydrous ether and 1 ml. of ethyl bromide add 39 g. of 3-dimethylaminopropyl chloride. While refluxing, add a solution of 20.9 g. of l-aza-l0,ll-dihydro-5H- dibenzo-[a,d]-cycloheptene-5-one in 100 ml. of ether and reflux the reaction mixture for 3 hours. Add 200 ml. of 100 percent ammonium chloride solution and extract with chloroform. Concentrate to a residue and recrystallize from ether obtaining the carbinol of this example, M.P. l06l09C.

The methods of Examples 1 and 2 are representative of the formation of the carbinols of Formula I, with Example 1 being applicable to all carbinols and especially preferred for the synthesis of those compounds wherein A represents N-methyl 4-piperidyl. Tetrahydrofuran has greater application as a solvent in these Grignard reactions and permits the use of higher concentrations. These reactions are not satisfactorily applicable to the preparation of carbinols of Formula I having less than three carbon atoms separating the amino group of A from the 5-position of the tricyclic nucleus.

' It is evident that any Grignard reagent bearing the substituents A, with the foregoing limitation, may be prepared in the usual manner described herein and sub stituted into the foregoing procecures to obtain the corresponding carbinol. Representative of such reagents, in addition to those described in Examples 1 and 2 are those wherein A represents: N-ethyl-4-piperidyl, N- methyl-S-piperidyl, 4-piperidyl, N-benzyl-4-piperidyl, di-lower alkylamino lower alkyl such as 3- dimethylaminopropyl, 4-dimethylaminobutyl, 3-(N- methyl-N-ethyl-amino)-propyl, S-dimethylaminopentyl, 8-dimethylaminooctyl, 4-dimethylaminocyclohexyl, 3-(4-dimethylaminocyclohexyl)-propyl, 4- dimethylaminocyclohexylmethyl, 3-pyrrolidinopropyl, 3-piperidinopropyl, 3-morpholinopropyl, 3-(4- methyl)-piperazinopropyl, 3-(4-(2-hydroxyethyl)piperazino)-propyl, 3-p-dimethylaminophenylpropyl, 3-diethylaminobutyl and the like.

It is also evident that any of the ketones, including the benzenoid substituted ketones, of Preparations A-D when substituted into Examples 1 and 2 with the Grignard reactants described above will give rise to the corresponding carbinol of Formula I.

In order to prepare carbinols of Formula I wherein A contains a primary of secondary amino group, such as 3-methylaminopropyl or 3-amin0propyl, the amino group is first protected by benzylation prior to formation of the Grignard reagent. Thus, utilizing the procedure of Example 2, one would react, for example, 3-(N-methyl-N'benzylamino )-propylmagnesium chloride with the appropriate ketone. subjecting the carbinol so formed to catalytic debenzylation by methods well known in the art affords the corresponding primary of secondary amine derivative. A similar transformation isapplicable to the preparation of carbinols of Formula I wherein A represents 4-piperidyl, the reactant being N-benzyl-4-piperidylmagnesium chloride.

It has been stated herein that the substituent A may be a group such as piperazino-lower alkyl or N-hydroxy-ethylpiperazino-lower alkyl and the like. These are prepared from a reagent such as 3-piperazinopropylmagnesium chloride or N -benzylpiperazinopropylmagnesium chloride followed by transformation of the N-benzyl or N--I-l group to the appropriately substituted moiety by methods well known in the art.

Following the methods taught by Examples 1 and 2, and utilizing knowledge ascribed to one skilled in the art, the following carbinols are prepared from the reaction of the appropriate ketone and appropriate Grignard reagent (in the following listing, for the sake of brevity, the phrase 10,1 l-dihydro-SH- dibenzo[a,d]cycloheptene-5-ol" is written as dihydrocarbinol while the 10,1 l-unsaturated analog is written as -carbinol. Accordingly, in this abbreviated nomenclature the compound of Example 1 would be written as 4-aza-5(N-methyl-4rpiperidyl)-dihydrocarbinol): 4-aza-5-(4-piperidyl)-dihydrocarbinol, 4 -aza-5- (N-benzyl-4-piperidyl)-dihydrocarbinol, 4-aza-5-(N- methyl-4-piperidyl)-dihydrocarbinol, 4-aza-5(3- dimethylaminopropyl)-dihydrocarbinol, 4-aza-5-(3- pyrrolidinopropyl)-dihydrocarbinol, 4-aza-5-(4- dimethylaminocyclohexylmethyl)-dihydrocarbinol, 4- aza-S 3-methylaminopropyl )-dihydrocarbinol, 4-aza- 5 3-dimethylaminobutyl)-dihydrocarbinol, 4-aza-5-( 3 -diethylarninoproifi wthhydrocarbinol, 4 aza-5 -(3 (4- methylpiperazino )propyl)-dihydrocarbinol, 4-aza-5-( 3 4-( Z-hydroxyethyl )piperazino )propyl )-dihydrocarbinol 4-aza-5-( 3 -methylbenzylamino )propyl dihydrocarbinol, 4-aza-5-( 2-methyl- 3dimethylaminopro pyl)-dihydrocarbinol, 4 -aza-5 2- methyl-3-methylaminopropyl)-dihydrocarbinol, 4-aza- 5-( 4-piperidyl)-carbinol, 4-aza-5 -(N-benzyl-4- piperidyl)-carbinol, 4-aza-5 -(N-methyl-4-piperidyl carbinol, 4-aza-5 3-dimethylaminopropyl )-carbinol 4-aza-5 3 -pyrrolidin opropyl )-carbinol, 4-aza-5-( 4- dimethylaminocyclohexylmethyl)-carbinol, 4-aza-5-( 3- methylaminopropyl)-carbinol, 4-aza-5 3 dimethylaminobutyl )-carbinol 4-aza-5 3- diethylaminopropyl )-carbinol, 4-aza-5 3 (4-methylpiperazino)propyl)-carbinol, 4-aza-5-(3-(4-(2-hydroxyethyl)piperazino)propyl)-carbinol, 4-aza-5-(3- (methylbenzylamino)propyl)-carbinol, 4-aza-5-(2- methyl-3-dimethylamino)propyl)-carbinol, 4-aza-5-(2- methyl-3-methylaminopropyl)-carbinol and the l-aza, 2-aza-, and 3-aza-analogs of the foregoing, as well as their 7-chloro, 7-trifluoromethyl, 8-chloro, 8-methyl-, 9-methyl-, 7-bromo-, 6-methoxyand 7-methyl-derivatives.

PREPARATION OF UNSATURATED COMPOUND BY DEHYDRATION OF CARBINOLS Example 3. 4-aza-5-(N-methyl-4-piperidylidene)- 10,11-dihydro-H-dibenzo[a,d]-cycloheptene Heat 5.4 g. of the carbinol of Example 1 and 270 g. of polyphosphoric acid for 12 hours at 140-170C. Pour into ice water and make alkaline with sodium hydroxide. Extract with ether. Dry ether solution and concentrate to a residue. Crystallize from isopropyl ether, M.P. 124-l26C. Example 4. 1-aza-5(3-dimethylaminopropylidene)- 10,11-dihydro-5H-dibenzo-[a,d]-cycloheptene Reflux for 8 hours a mixture of 14 g. of carbinol of Example 2, 160 ml. of glacial acetic acid and 50 ml. of concentrated hydrochloric acid. Concentrate to a residue in vacuo, make alkaline and extract with chloroform. Concentrate the chloroform solution to a residue and distil, collecting that fraction boiling at 175-180C./l mm.

PREPARATION OF UNSATURATED COMPOUNDS HAVING A Z-CARBON CHAIN Example 5. 4-aza-5-(3-dimethylaminoethylidene)- 10,1 1-dihydr0-5H-dibenzo-[a,d]-cycloheptene Step 1. To a stirred mixture of 13 g. zinc (20 mesh), 33.4 g. of ethyl bromoacetate in 400 ml. of benzenetoluene (1:1), add, dropwise, a solution of41.4 g. of 4- aza-10,1 1-dihydro-5H-dibenzocycloheptene-5-one. Heat for 2 hours on a steam bath, add 13 g. zinc and continue heating for 4 hours. Cool, add 10 percent acetic acid and separate layers. Extract aqueous phase with benzene and combine benzene fractions. Concentrate to a residue and distil in vacuo obtaining 4-aza-5- carbethoxymethyl-10,l l-dihydro-5H-dibenzo[a,d] cycloheptene-S-ol.

.Step 2. Dehydrate the carbinol of step 1 by heatingat -100C. 20 g. of the carbinol with ml. of acetic anhydride containing 1-2 percent sulfuric acid. After 3 hours, concentrate in vacuo, dilute with water, neutralize and extract with ether. Concentrate to a residue and distil in vacuo to obtain 4-aza-5-carbethoxymethylidene-10,1 l-dihydro-5H-dibenzo-[a,dl-cycloheptene. Step 3. Reflux 15 g. of the methylidene compound from step 2 with 15 g. potassium hydroxide, 50 ml. water and ml. ethanol for 6 hours on a steam bath. Concentrate to a residue, add water and extract with ether. Neutralize aqueous layer with acetic acid and allow product to crystallize. Filter and recrystallize from aqueous methanol obtaining 4-aza-5-(carboxymethylidene-l 0,1 1-dihydro-5H-dibenzo-[a,d]- cycloheptene.

Step 4. Reflux 12 g. of the acid from step 3 with 50 ml. of thionyl chloride. Concentrate in vacuo, add 50 ml. of benzene and evaporate to a residue. Take up in 150 ml. of benzene and while stirring add a solution of 9 g. of dimethylamine in benzene. Stir and reflux for 4 hours and then pour into water. Make alkaline with sodium carbonate and extract with benzene. Concentrate in vacuo to obtain 4-aza-5-dimethylcarboxamido- 10,11-dihydro-5I-I-dibenzocycloheptene. Purify by recrystallization from methanol.

Step 5. Add an ether solution of 10 g. of the amide from step 4 to a suspension of 3 g. of lithium aluminum hydride in 250 ml. of ether. Stir for 2 hours, add water and separate layers. Concentrate ether to a residue obtaining 4-aza-5-dimethylaminoethylidene-10,1 ldihydro-SH-dibenzocycloheptene. Purify by distillation in vacuo.

All of the carbinols described heretofore when subjected to the dehydration methods of Examples 3 and 4, or obvious equivalents thereof give rise to the corresponding exocyclic unsaturated product. The procedure of Example 5 is used to prepare ethylidene compounds of Formula I. Representative of the unsaturated compounds prepared by these methods and their equivalents are those listed below wherein the abbreviated nomenclature described heretofore is again employed with the modification that carbinol is dropped in favor of heptene, thus the compound of Example 3 is described by this appreviation as 4-aza- 5(N-methyl-4-piperidylidene )-dihydro-heptene: 3-aza-5-(4-piperidylidene)-dihydroheptene, 3-aza-5- (n-benzyl-4-piperidylidene)-dihydroheptene, 3-aza-5- (N-methyl-4-piperidylidene)-dihydroheptene, 3-aza-5- (3-dimethylaminopropylidene)-dihydroheptene, 3-aza- 5 3-pyrrolidinopropylidene )-dihydroheptene 3 -aza- 5-(4-dimethylaminocyclohexylmethylidene)- dihydroheptene, 3-aza-5-( 3-methylaminopropylidene)- dihydroheptene, 3-aza-5-(3-dimethylaminobutylidene )-dihydroheptene, 3 -aza-5 3- diethylaminopropylidene)-dihydroheptene, 3-aza-5-[ 3- (4-methylpiperazino)-propylidene]-dihydroheptene, 3- aza-5-[3-(4-(2-hydroxyethyl)piperazino)propylidene]- dihydroheptene, 3-aza-5-[3-(methylbenzylamino)propylidene]-dihydroheptene, 3-aza-5-[ (2-methyl-3-dimethylamino)propylidene]-dihydroheptene, 3-aza-5-[(2-methyl-3-methylamino)propylidene] -dihydroheptene, 3-aza-5-(2-dimethylaminoethylidene)-dihydroheptene, 3l-aza-5-(2 pyrrolidinoethylidene )-dihydroheptene, 3-aza-5-(2- dibenzylaminoethylidene)-dihydroheptene, 3-aza-5-(4- piperidylidene )-heptene, 3-aza-5-(N-benzyl-4- piperidylidene )-heptene, 3-aza-5 -(N-methyl-4- piperidylidene)-heptene, 3-aza-5-( 3- dimethylaminopropylidene)-heptene, 3-aza-5-(3-pyrrolidinopropylidene)-heptene, 3-aza-5-(4- dimethylaminocyclohexylmethylidene)-heptene, aza-5-(3-methylaminopropylidene)-heptene, (3-dimethylaminobutylidene)-heptene, diethylaminopropylidene)-heptene, 3-aza-5-[3(4- rnethyl-piperazino)propylidene]-heptene, 3-aza-5-[ 3- (4-2-hydroxyethyl)piperazino)propylidene]heptene, 3- aza-5-[3-(methylbenzylamino)propylidene]-heptene, 3-aza-5-[(2-methyl-3-dimethylamino)propylidene]- heptene, and the l-aza, 2-aza and 4-aza analogs of the foregoing, as well as their 7-chloro, 7-trifluoromethyl,

PREPARATION OF SATURATED COMPOUNDS Example 6. l-aza-S 3 -dimethylaminopropyl)- 10 ,l 1 -dihydro-5 I-I-dibenzo a,d -cyclohept ene piperidyU-heptene, v heptene, l aza-S-(N -methyl 4-piperidyl)-heptene, 1-

Hydrogenate in a Parr shaker a solution of 6.8 g. of the compound of Example 4 in 100 ml. of ethanol in the presence of 0.5 g. of platinum oxide under about 50 lbs. pressure of hydrogen until an equivalent quantity of hydrogen is absorbed. Filter and concentrate the filtrate to a residue and distil collecting that fraction boiling at l65l70/1 mm.

This method is generally applicable to the preparation of the saturated compounds of Formula I which are also saturated at the 10,1 l-position. The catalytic hydrogenation will generally reduce a lO,l l-double bond and thus to prepare such l0,l l-unsaturated compounds, the method of Example 7 is applicable. Example 7. 4-aza-5-(dimethylaminoethyl)-5H- dibenzo[a,d]-cycloheptene Add 18.2 g. of 4-aza-5H-dibenzo[a,d]-cycloheptene (Preparation E) to a solution of sodamide (from 2.5 g. of sodium) in 200 ml. of anhydrous ammonia. Stir for 2 hours and then add slowly 10.7 g. .of dimethyl aminoethyl chloride. After 1 hour displace the ammonia with ether and then reflux for 6-8 hours. Pour into ice.water and extract with ether. Concentrate to a residue and distil in vacuo to obtain the compound of this example.

This method is applicable to the preparation of al the saturated" compounds of Formula I, the l0,l ldihydro as well as the unsaturated analogs thereof.

Saturated compounds of Formula I, prepared by the methods of Examples 6 and 7, or obvious,

equivalents thereof are. set forth in the following representative listing with the abbreviated nomenclature employed as before: laza--(4-p iperidyl)- aza- 5-( B-dimethylaminopropyl )-heptene, l-aza-5-( 3- pyrrolidinopropyl )-heptene, l-aza-5-( 4- dimethylaminocyclohexylmethyl )-heptene l-aza-5-( 3- methylaminopropyl )-heptene, l-aza-5-( 3- dimethylaminobutyl )-heptene, l-aza-S 3- diethylaminopropyl )-heptene l-aza-5-[ 3 (4-methylpiperazino )propyl ]-heptene, l-aza-5-[ 3-( 4-( 2-hydroxyethyl) piperazino )propyl ]-heptene l-aza-S 3 (methylbenzylamino )propyl] l-aza-5-( 2- methyl-3-dimethylamino-propyl )-heptene l-aza-S 2- methyl- 3-methylamino-propyl)-heptene, l-aza-S 2- dimethylaminoethyl )-heptene, l-aza-5-( 2-pyrrolidinoethyl )-heptene, l-aza-S 2- dibenzylammoethyl)-heptene, and the 2-aza-, 3-aza-, and 4-aza analogs of the foregoing. as well as their 7- chloro-7-trifluoromethyl, 8-methyl-, 9-methyl-, 7- brorno-, 6-methoxyand 7-methylderivatives.

PREPARATION OF PHARMACEUTICAL SALTS dimaleate, M.P. l52-154C.

dihydroheptene, l-aza-S-( N-benzyl-4-piperidyl v dihydroheptene, l-aza-5-( N -meth yl-4-piperidyl dihydroheptene, l-aza-5-( 3-dimethylaminopropyl dihydroheptene, 1-aza-5-( 3-pyrrolidinopropyl dihydroheptene, l-aza-S 4-dimethyl am inocyclohexylmethyl)-dihydroheptene, l-aza-S-(3- methylaminopropyl)-dihydroheptene, l-aza-5-(3- dimethylaminobutyl)-dihydroheptene, l-aza-5-(3- diethylaminopropyl)-dihydroheptene, l-aza-5-[ 3(4- methylpiperazino)propyl]-dihy'droheptene, l-aza-5-[3- climethylaminoethyl)-dihydroheptene, l-aza-5-(2-pyrrolidinoethyl)-dihydroheptene, dibenzylaminoethyl )-dihydroheptene,

chloro.

trifluoromethyl.

I claim: 1. A member selected from the, group consisting of a compound having the'formula:

wherein Q is a member selected from the group consisting of lower loweralkoxy, halogen or trifluoromethyl.

2. A compound of claim 1 wherein Q represents halogen.

3. A. compound of claim 1 wherein the halogen is 4. A compound of claim I wherein "Q is 5. A compound of claim 3 wherein chloro is'located' at the 3-position of the phenyl moiety. a x i 

1. A member selected from the group consisting of a compound having the formula: wherein Q is a member selected from the group consisting of lower loweralkoxy, halogen or trifluoromethyl.
 2. A compound of claim 1 wherein Q represents halogen.
 3. A compound of claim 1 wherein the halogen is chloro.
 4. A compound of claim 1 wherein Q is trifluoromethyl. 